Pharmacologic Interventions for AddictionsMost common side effects: skin reactions, headache,...
Transcript of Pharmacologic Interventions for AddictionsMost common side effects: skin reactions, headache,...
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Pharmacologic Interventions for
Addictions
Eric C. Strain, M.D.Johns Hopkins University School of Medicine, Baltimore, Maryland
Maryland Psychiatric SocietyNovember 7, 2015
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Objectives for This Talk
I. Identify at least two FDA-approved medications used for the treatment of alcohol use disorders
II. Identify at least three FDA-approved medication formulations used for the treatment of nicotine use disorders
III. Identify at least one new medication that is currently under development for the treatment of an addictive disorder
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Outline for This Talk
I. Drug classes and medications currently approved for their treatment
II. Medications under development
III. Summary and conclusions
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A Caveat
Focusing today on medications for the treatment of these disorders, but important to note that non-pharmacological interventions play a critical role in the treatment of these disorders. Just as we talk of “dose-related” efficacy of medications, there can also be a dose-related efficacy of non-pharmacological services.
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Effect of Counseling in Methadone Treatment
(McLellan et al., 1993)
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Outline for This Talk
I. Drug classes and medications currently approved for their treatment
II. Medications under development
III. Summary and conclusions
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Drug Classes and Approved Medications
A. Alcohol
B. Nicotine
C. Opioids
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Drug Classes and Approved Medications
Will focus on these three drug classes (approved medications):
A. Alcohol
B. Nicotine
C. Opioids
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Alcohol pharmacological treatments
Disulfiram – 1950s
Naltrexone (oral, alcohol) – 1995
Acamprosate – Europe 1989; U.S. 2004
Naltrexone (extended release, alcohol) – 2006
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Trade name: Antabuse; FDA approved in 1951
Blocks aldehyde dehydrogenase; causes increase in acetaldehyde when person drinks (with subsequent disulfiram-alcohol reaction)
Reaction starts within 30 minutes of drink; can consist of flushing, sweating, throbbing, N/V, increased HR, weakness; can be severe in some cases
Disulfiram
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Don’t start until at least 12 hours of abstinence
Dose range: 125-500 mg once per day (average, 250 mg/day)
Works best if compelling reason to take it
Disulfiram
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Risk considerations:
Can have a disulfiram-alcohol reaction (do not use in persons with cardiac disease)
Most common side effects: skin reactions, headache, drowsiness/fatigue, impotence, garlic taste
Rarely hepatic toxicity, neurologic reactions
Disulfiram
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Risk considerations:
Can use in persons with liver disease if liver function tests okay (<5x ULN) – monitor LFTs
Need to watch for alcohol-containing products (mouthwash, sauces, lotions)
Disulfiram
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Bottom line with disulfiram:
Generally a safe medication, biggest concerns are probably liver function tests/liver disease, risk of patient drinking while taking it, and compliance with taking it
Disulfiram
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Evolution of alcohol pharmacological treatments
Disulfiram – 1950s
Naltrexone (oral, alcohol) – 1995
Acamprosate – Europe 1989; U.S. 2004
Naltrexone (extended release, alcohol) – 2006
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Trade name: ReVia, Depade, others
Opioid antagonist
Mechanism of efficacy when used to treat alcoholism is not clear
Efficacy studies show better outcomes vs. placebo -- decreases craving; improves relapse rates (and longer time to relapse), lower percentage of drinking days and fewer drinks on days the person did drink
Naltrexone (oral)
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Recommended 3-7 days abstinence before start
Typical dose: 50 mg per day (but, higher doses may be more effective -- up to 150 mg per day)
Naltrexone (oral)
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Risk considerations:
Generally well tolerated medication with no significant side effects
In some cases can see some side effects: GI (nausea, vomiting), headache, fatigue, nervousness, headache, rash
Label warns regarding hepatotoxicity (black box) – an unfortunate situation, not really relevant
Naltrexone (oral)
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Other considerations:
Watch use if liver or renal impairment
Need to stop if planning major surgery (possible need for opioid analgesics)
Can have drug interactions
Naltrexone (oral)
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Bottom line with naltrexone:
Generally a safe medication and consistent evidence that it is effective
Hepatoxicity not a substantial problem
Nausea/GI effects can be seen
Biggest drawback is cannot use if opioid agonists needed
Naltrexone (oral)
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Disulfiram
Disulfiram – 1950s
Naltrexone (oral, alcohol) – 1995
Acamprosate – Europe 1989; U.S. 2004
Naltrexone (extended release, alcohol) – 2006
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Trade name: Campral; FDA approved in 2004, but used for years in Europe
Mechanism of action not clear (glutamate?)
Not metabolized by the liver; do need to reduce dose if renal impairment
Use: 666 mg three times per day
Do not crush tablets
Acamprosate
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Begin several days after last drink
Efficacy of some debate; two U.S. studies failed to show better results than placebo
May be useful in patients with higher motivation, possibly with more severe dependence
Acamprosate
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Risk considerations:
Safe medication
No risk of abuse
Virtually no overdose risk
Minimal side effects (diarrhea)
Few drug interactions (can increase naltrexone blood levels)
Acamprosate
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Risk considerations:
Can be used in patients with liver disease (not hepatic metabolism)
Can be used with opioids (e.g., methadone, buprenorphine treated patients)
Acamprosate
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Bottom line with acamprosate:
May be useful under certain circumstances, and risk profile is an advantage to this medication
Acamprosate
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Disulfiram
Disulfiram – 1950s
Naltrexone (oral, alcohol) – 1995
Acamprosate – Europe 1989; U.S. 2004
Naltrexone (extended release, alcohol) – 2006
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Trade name: Vivitrol; FDA approved in 2006
Opioid antagonist
Similar features as oral naltrexone
Administered as gluteal injection given (380 mg) given once every four weeks
Naltrexone (extended release)
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While similar profile as that seen with oral naltrexone, advantage in compliance (which has been shown to be an important factor in outcome for naltrexone treatment)
Naltrexone (extended release)
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Risk considerations and bottom line:
Similar concerns as with oral naltrexone
Can see injection site reactions, infrequently depression
Important consideration is whether there is a need to use opioids in weeks after receiving an injection
Naltrexone (extended release)
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Drug Classes and Approved Medications
A. Alcohol
B. Nicotine
C. Opioids
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Nicotine pharmacological treatments
Nicotine -- gum ‘84; patch ‘92; nasal spray ‘96; inhaler ’97
Bupropion – 1997
Varenicline -- 2006
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Nicotine
Nicotine gum initially approved as a prescription product (1984); made available over the counter (OTC) in 1996
Followed by other nicotine delivery systems (patch [by prescription, 1992; OTC 1996], nasal spray [prescription only, 1996], inhaler [prescription only, 1997])
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Nicotine
NRT = nicotine replacement therapy
NRT products generally safe, more effective than placebo (multiple studies have shown, conclusion of Cochrane review), using 6 months sustained/prolonged abstinence after start of treatment
OR of 1.84 (1.71-1.99)
Combinations of NRT outperform NRT alone
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Nicotine
Overall safety profile good – can see some minor concerns (for example, skin reactions with patch, hiccups with gum)
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Nicotine pharmacological treatments
Nicotine -- gum ‘84; patch ‘92; nasal spray ‘96; inhaler ’97
Bupropion – 1997
Varenicline -- 2006
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Bupropion
Bupropion initially marketed in U.S. as an antidepressant (Wellbutrin products)
Approved for smoking cessation (by prescription) in U.S. in 1997 (intriguing alternate mechanism of action -- not another nicotine-based product; grew out of clinical observation)
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Bupropion
Functions as a weak dopamine and norepinephrine reuptake inhibitor, and also appears to have some effects on nicotinic receptors
Efficacy is not related to its antidepressant effects
Marketed as Zyban (and need to ensure double dosing does not occur through prescribing of it for smoking cessation and for depression)
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Bupropion
Like NRT, more effective than placebo (OR 1.60, 95% 1.60-2.06 – similar to NRT, and not significantly different on head-to-head comparison)
Typically start dosing similar to use as an antidepressant (150 mg/d for several days, then increase to 300 mg/d), and set quit date after stabilized on medication (e.g., a week after dosing)
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Bupropion
Primary concern with risk of seizures, which is dose related, and can occur if other risk factors for seizures
Other effects possible (GI, headache)
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Nicotine pharmacological treatments
Nicotine -- gum ‘84; patch ‘92; nasal spray ‘96; inhaler ’97
Bupropion – 1997
Varenicline -- 2006
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Varenicline
Varenicline (Chantix, Champix) approved in U.S., 2006
Yet another mechanism of action (partial nicotinic agonist, vs. nicotine replacement products and antidepressant)
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Varenicline
Efficacy superior to NRT, bupropion
Compared to placebo: OR 2.88 (95%, 2.40-3.47)
Initial concerns of neuropsychiatric effects (depression, suicidal ideation) – these do not appear to be as great a concern as initially noted
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Varenicline
Dosing relatively simple (0.5 mg a day for 3 days, 0.5 mg twice a day; no more than 2 mg total per day)
Set quit date a week or so after start use
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Drug Classes and Approved Medications
A. Alcohol
B. Nicotine
C. Opioids
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Evolution of pharmacologic treatments Methadone – 1960sNaltrexone (oral, opioids) – 1984LAAM – 1993Buprenorphine – France 1996; U.S. 2002Naltrexone (extended release, opioids) – 2010
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Opioid treatments
Essentially two primary approaches:
Opioid agonist or partial agonists: have main therapeutic effect on mu receptor (activate it)
(Buprenorphine, LAAM, methadone)
Opioid antagonists: occupy opioid receptors (primary therapeutic target is mu receptor), but don’t activate the receptor
(Naltrexone)
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Opioid treatments
Essentially two delivery systems:
Opioid Treatment Programs (OTPs – what we would have called methadone clinics in the past)
(Buprenorphine, LAAM, methadone)
Office Based Opioid Treatment (OBOT)
(Buprenorphine, Naltrexone)
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Opioid treatments
All of these treatments are effective, safe
Substantial database supporting use of these medications
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Outline for This Talk
I. Drug classes and medications currently approved for their treatment
II. Medications under development
III. Summary and conclusions
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Potential new medications
Alcohol
Opioids
Cocaine/stimulants
Cannabis
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Ondansetron
Topiramate
Rimonabant
Quetiapine
Levetiracetam
Varenicline
Medications studied for alcoholism
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Ondansetron: approved for treatment of nausea; low doses useful for alcoholism, especially early-onset?
Topiramate
Rimonabant
Quetiapine
Levetiracetam
Varenicline
Medications studied for alcoholism
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Ondansetron
Topiramate: anticonvulsant, migraine treatment; clinical trials showing efficacy for alcoholism, but side effects may limit development
Rimonabant
Quetiapine
Levetiracetam
Varenicline
Medications studied for alcoholism
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Ondansetron
Topiramate
Rimonabant: cannabinoid antagonist briefly marketed outside U.S. for obesity but withdrawn (side effects); cannabinoid system remains of interest
Quetiapine
Levetiracetam
Varenicline
Medications studied for alcoholism
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Ondansetron
Topiramate
Rimonabant
Quetiapine: first medication studied by NIAAA’s clincial trial program (NCIG, “Get Control”)
Levetiracetam
Varenicline
Medications studied for alcoholism
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NCIG (NIAAA Clinical Investigations Group)
Multi-site program for studying new medications for alcohol dependence (Hopkins, Penn, UVA, Boston U, Dartmouth)
NCIG
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Ondansetron
Topiramate
Rimonabant
Quetiapine: no efficacy found for alcohol dependence
Levetiracetam
Varenicline
Medications studied for alcoholism
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Ondansetron
Topiramate
Rimonabant
Quetiapine
Levetiracetam: approved anticonvulsant; second medication studied in NCIG, and again no efficacy found for alcoholism
Varenicline
Medications studied for alcoholism
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Ondansetron
Topiramate
Rimonabant
Quetiapine
Levetiracetam
Varenicline: partial nicotinic agonist; approved for the treatment of nicotine dependence; recent NCIG study showing efficacy for alcoholism
Medications studied for alcoholism
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Varenicline
200 subjects randomized (198 analyzed); alcohol dependent, but not needing medically supervised withdrawal
13 week trial
Target varenicline dose of 1 mg bid
Concurrent computer-based treatment
Medications studied for alcoholism
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Varenicline for alcohol dependence
Litten et al., JAM, 2013)
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Varenicline for alcohol dependence
Primary outcome:PercentHeavyDrinkingDays(HDD)
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Varenicline for alcohol dependence
Varenicline
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Varenicline
Intriguing results
Medications studied for alcoholism
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Potential new medications
Alcohol
Opioids
Cocaine/stimulants
Cannabis
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Medications studied for opioid dependence
Lofexidine
Buprenorphine rods
Buprenorphine injections
Other buprenorphine products
Tramadol
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Potential new medications
Alcohol
Opioids
Cocaine/stimulants
Cannabis
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Medications studied for cocaine/stimulants
Naltrexone: opioid antagonist; no evidence of efficacy for cocaine or methamphetamine, but interesting results for amphetamine dependence
Cocaine vaccine
Modafinil
Disulfiram
Amphetamine products
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Medications studied for cocaine/stimulants
80 amphetamine-dependent patients; double-blind, RCT(Jayaram-Lindstrom et al., AJP, 2008)
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Medications studied for cocaine/stimulants
Naltrexone
Cocaine vaccine: cocaine bound with protein (cholera toxin), creates antibodies -- prevents cocaine from then crossing blood brain barrier
Modafinil
Disulfiram
Amphetamine products
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Medications studied for cocaine/stimulants
Naltrexone
Cocaine vaccine
Modafinil: treatment for narcolepsy, excessive sleepiness; clincial trials for cocaine have been equivocal (some positive, but not all), and some suggestion that persons with higher levels of methamphetamine dependence may respond
Disulfiram
Amphetamine products
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Medications studied for cocaine/stimulants
Naltrexone
Cocaine vaccine
Modafinil
Disulfiram: initially studied for dual alcohol/cocaine users (10+ years ago), but then studies found effective without alcohol use; results for positive effect less consistent over time; may need a champion to push it forward
Amphetamine products
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Medications studied for cocaine/stimulants
Naltrexone
Cocaine vaccine
Modafinil
Disulfiram
Amphetamine products: studies as a proof of concept (for cocaine), have shown can work
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Medications studied for cocaine/stimulants
82 cocaine-dependent patients; double-blind, RCT
Tested methamphetamine (immediate release and sustained release)
(Mooney et al., DAD, 2009)
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Medications studied for cocaine/stimulants
SR methamphetamine group (30 mg once a day) – lowest rates of cocaine + urine samples over time
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Potential new medications
Alcohol
Opioids
Cocaine/stimulants
Cannabis
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Medications studied for cannabis
Dronabinol: approved form of delta-9-THC (nausea, vomiting, weight gain); CB-1 agonist, and use follows logic of other agonist treatments; evidence from clinical pharmacology studies that may be effective in treating cannabis withdrawal
Zolpidem
(Rimonabant)
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156 cannabis dependent patients (RCT)
Dronabinol associated with better treatment retention
(Levin et al., DAD, 2011)
Medications studied for cannabis
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Dronabinol decreased cannabis withdrawal
(Levin et al., DAD, 2011)
Medications studied for cannabis
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Medications studied for cannabis
Dronabinol
Zolpidem: approved medication for insomnia; logic of it is to treat a prominent symptom of cannabis withdrawal (sleep difficulties)
(Rimonabant)
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Cannabis withdrawal (DSM-5)
Three or more of the following:1. Irritability, anger, or aggression
2. Nervousness or anxiety
3. Sleep difficulty (e.g., insomnia, disturbing dreams)
4. Decreased appetite or weight loss
5. Restlessness
6. Depressed mood
7. At least one of the following physical symptoms causing significant discomfort: abdominal pain, shakiness/tremors, sweating, fever, chills, or headache
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Medications studied for cannabis
Dronabinol
Zolpidem: evidence that there are increasing numbers of persons seeking treatment for cannabis dependence, and who report difficulty stopping cannabis use (related, in part, to sleep problems associated with withdrawal)
(Rimonabant)
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Medications studied for cannabis
Cannabis
Zolpidem
(Rimonabant: cannabinoid antagonist, and such antagonists are theoretically interesting as possible therapeutic options for treating cannabis dependence)
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Outline for This Talk
I. Drug classes and medications currently approved for their treatment
II. Medications under development
III. Summary and conclusions
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Summary of potential new medications
The primary driver behind medication development for substance use disorders has been (and will probably continued to be) NIH; the pharmaceutical companies have picked up interest in addictions, but primarily in forms of buprenorphine
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Summary/conclusions
Progress in the development of medications for treatment drug use disorders, although after a burst of work in late 1990s/early 2000s, seems there has been some decrease in the pace of novel pharmacotherapies
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Summary/conclusions
While emphasis here is on medications, want to stress that efficacy of these medications is enhanced when combined with effective non-pharmacologic treatments
True advances may require the identification of new mechanisms for medications actions (such as vaccines or facilitation of learning) – it may be that the current pharmacological approaches are less fruitful (the agonist models of therapies)
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Summary/conclusions
In addition to the development of medications, we are witnessing considerable change in the organization and reimbursement of substance abuse treatment, and this has the potential to lead to need for expanded treatment capacity
Finally, we are also witnessing a social experiment with respect to cannabis – some might say an ironic twist to the current cultural disdain for smoking tobacco
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Thank you
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Acknowledgements
Support of the National Institute on Drug Abuse (K24 DA023186)